ClinVar Miner

Submissions for variant NM_170682.4(P2RX2):c.1037C>G (p.Ala346Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV002512502 SCV002773888 uncertain significance Autosomal dominant nonsyndromic hearing loss 41 2022-06-23 criteria provided, single submitter clinical testing

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